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由烷硫醇单分子层中疏水相互作用驱动的自组装:混合双层膜的形成机制。

Self assembly driven by hydrophobic interactions at alkanethiol monolayers: mechanisms of formation of hybrid bilayer membranes.

作者信息

Hubbard J B, Silin V, Plant A L

机构信息

Biotechnology Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

出版信息

Biophys Chem. 1998 Dec 14;75(3):163-76. doi: 10.1016/s0301-4622(98)00199-9.

Abstract

The mechanism for the formation of biomimetic model cell membranes consisting of bilayers composed of alkanethiols and phospholipids was probed with a kinetic study using surface plasmon resonance. The kinetics of formation of a monolayer of phospholipid from vesicles in solution onto a hydrophobic alkanethiol monolayer is described by a model that takes into account the lipid concentration, diffusion, and a surface reorganization rate constant. Monomer phospholipid apparently does not play a direct role in determining the kinetics of bilayer formation. Expressions for the limiting cases of this model describe the behavior of two distinct vesicle concentration conditions. At high concentrations of lipid vesicles the formation of the bilayer appears to be limited by the diffusion of vesicles to the surface; at lower concentrations of vesicles, the rate-limiting step is apparently the surface reorganization of lipid. This kinetic model can also be used to describe the formation of a biomimetic bilayer from an alkanethiol monolayer and cell membranes.

摘要

利用表面等离子体共振进行动力学研究,探究了由烷硫醇和磷脂组成的双层仿生模型细胞膜的形成机制。溶液中的脂质体在疏水烷硫醇单层上形成磷脂单层的动力学过程,可用一个考虑脂质浓度、扩散和表面重组速率常数的模型来描述。单体磷脂在决定双层形成动力学方面显然不发挥直接作用。该模型极限情况的表达式描述了两种不同脂质体浓度条件下的行为。在高浓度脂质体时,双层的形成似乎受脂质体向表面扩散的限制;在较低脂质体浓度下,限速步骤显然是脂质的表面重组。该动力学模型还可用于描述由烷硫醇单层和细胞膜形成仿生双层的过程。

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